Please choose an event type to view the corresponding MedsFacts report:

ALANINE AMINOTRANSFERASE INCREASED ( 27 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
CARDIAC FAILURE ( 24 FDA reports)
DYSPNOEA ( 21 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 15 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
BLOOD BILIRUBIN INCREASED ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
VOMITING ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
ATRIAL FIBRILLATION ( 12 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
HYPOTENSION ( 11 FDA reports)
ECZEMA ( 10 FDA reports)
FALL ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
TOXIC SKIN ERUPTION ( 9 FDA reports)
COAGULOPATHY ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
MALAISE ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CEREBRAL HAEMATOMA ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
COUGH ( 4 FDA reports)
DECEREBRATION ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PAIN ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SUICIDAL BEHAVIOUR ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COMA ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
WOUND ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PULMONARY ARTERY ANEURYSM ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACANTHOLYSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERAL ANAESTHESIA ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART AND LUNG TRANSPLANT ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 1 FDA reports)
ODONTOGENIC CYST ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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